Synthesis of some new azoles and their fused derivatives with anticipated biological activity / Doha Samir Mohamed Okpy ; Supervised Mohamed Ahmed Badawy , Nadia Hanafy Metwally ,
Material type:
- تشييد بعض الأزولات الجديدة ومشتقاتها الملتحمة ذات نشاط بيولوجى متوقع [Added title page title]
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Item type | Current library | Home library | Call number | Copy number | Status | Barcode | |
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.12.10.M.Sc.2014.Do.S (Browse shelf(Opens below)) | Not for loan | 01010110064015000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.12.10.M.Sc.2014.Do.S (Browse shelf(Opens below)) | 64015.CD | Not for loan | 01020110064015000 |
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Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry
The original work of this thesis includes TWO research parts: The first part:- Studies the reactions of 5-ethoxymethylene-2-thioxo-4-thiazolidinone with ethyl glycinate and ethyl hydrazine carboxylate to afford imidazo[2,1-b]thiazoledione derivative and hydrazine carboxylate derivative of 2-thioxo-4-thiazolidinone respectively. The condensation of 5-(amino-methylene)-2-thioxo-4-thiazolidinone with different aromatic aldehydes in presence of piperidine as a basic catalyst afforded Z-5-(piperidin-1-ylmethylene)-2-thioxo-4-thiazolidinone. The alkaline hydrolysis of 5-aryl methylene)-2-thioxo-4-thiazolidinone affords 3-aryl-2-mercaptoacrylic acid derivatives, the latter compounds react with different {uF061}-arylhydrazono-malononitriles and trichloroacetonitrile to afford the corresponding thiazole derivatives. The structure for selected compounds was confirmed by X-ray crystallography
Issued also as CD
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